A Study of cryostructuring of polymer systems. 41. Complex and composite poly(vinyl alcohol) cryogels containing soluble and insoluble forms of chitosan, respectively
- Authors: Podorozhko E.A.1, Ul’yabaeva G.R.2, Kil’deeva N.R.2, Tikhonov V.E.1, Antonov Y.A.3, Zhuravleva I.L.3, Lozinsky V.I.1
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Affiliations:
- Nesmeyanov Institute of Organoelement Compounds
- Moscow State University of Design and Technology
- Emanuel Institute of Biochemical Physics
- Issue: Vol 78, No 1 (2016)
- Pages: 90-101
- Section: Article
- URL: https://journal-vniispk.ru/1061-933X/article/view/200178
- DOI: https://doi.org/10.1134/S1061933X16010130
- ID: 200178
Cite item
Abstract
Complex macroporous poly(vinyl alcohol) (PVA) cryogels have been obtained by cryogenic treatment (freezing at–20°C for 12 h followed by defrosting at a rate of 0.03°C/min) of PVA–chitosan hydrochloride mixed solutions. The subsequent alkaline treatment of the cryogels has resulted in the transformation of the water-soluble salt form of chitosan into its insoluble basic form, which coagulates inside the bulk of the continuous phase of PVA cryogel into small particles with sizes of 2–5 µm. In the resulting composite cryogels, these particles play the role of an “active” filler, which increases the rigidity and heat endurance of the gel material. It has been shown that the sorption capacity of such chitosan particles entrapped into the bulk of composite cryogels with respect of bivalent copper ions is noticeably higher than the sorption capacity of ground chitosan particles incorporated as a discrete filler into the continuous phase PVA cryogels. The study of the properties of PVA–chitosan hydrochloride mixed solutions revealed that these polymers are, to a large extent, compatible with one another in a common solvent at a low ionic strength. Therefore, liquidliquid phase separation of these systems due to the thermodynamic incompatibility of macromolecules of different natures is observed only upon increasing the ionic strength by adding a low-molecular-mass salt (NaCl, 0.15 mol/L) to the solution.
About the authors
E. A. Podorozhko
Nesmeyanov Institute of Organoelement Compounds
Email: loz@ineos.ac.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991
G. R. Ul’yabaeva
Moscow State University of Design and Technology
Email: loz@ineos.ac.ru
Russian Federation, ul. Sadovnicheskaya 33/1, Moscow, 117997
N. R. Kil’deeva
Moscow State University of Design and Technology
Email: loz@ineos.ac.ru
Russian Federation, ul. Sadovnicheskaya 33/1, Moscow, 117997
V. E. Tikhonov
Nesmeyanov Institute of Organoelement Compounds
Email: loz@ineos.ac.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991
Yu. A. Antonov
Emanuel Institute of Biochemical Physics
Email: loz@ineos.ac.ru
Russian Federation, ul. Kosygina 4, Moscow, 119991
I. L. Zhuravleva
Emanuel Institute of Biochemical Physics
Email: loz@ineos.ac.ru
Russian Federation, ul. Kosygina 4, Moscow, 119991
V. I. Lozinsky
Nesmeyanov Institute of Organoelement Compounds
Author for correspondence.
Email: loz@ineos.ac.ru
Russian Federation, ul. Vavilova 28, Moscow, 119991
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